HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver, CO 80239, NDC: 73177-0104-05.
Reported: February 23, 2022 Initiated: February 3, 2022 #D-0633-2022
Product Description
HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver, CO 80239, NDC: 73177-0104-05.
Reason for Recall
Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A
Details
- Recalling Firm
- STAQ Pharma, Inc.
- Units Affected
- 905 Syringes
- Distribution
- CO, OH, and TX.
- Location
- Denver, CO
Frequently Asked Questions
What product was recalled? ▼
HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver, CO 80239, NDC: 73177-0104-05.. Recalled by STAQ Pharma, Inc.. Units affected: 905 Syringes.
Why was this product recalled? ▼
Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 23, 2022. Severity: Critical. Recall number: D-0633-2022.
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